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TITLE: High frequency of CHD7 mutations in congenital hypogonadotropic hypogonadism  Full Text
AUTHORS: Gonçalves, CI; Patriarca, FM; Aragüés, JM; Carvalho, D ; Fonseca, F; Martins, S; Marques, O; Pereira, BD; Martinez de Oliveira, J; Lemos, MC;
PUBLISHED: 2019, SOURCE: Scientific Reports, VOLUME: 9, ISSUE: 1
INDEXED IN: Scopus CrossRef: 16
IN MY: ORCID
22
TITLE: UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries
AUTHORS: Lorigo, M; Quintaneiro, C; Lemos, MC; Martinez de Oliveira, J; Breitenfeld, L; Cairrao, E;
PUBLISHED: 2019, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 20, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 13
IN MY: ORCID
23
TITLE: Combined Pituitary Hormone Deficiency Caused by a Synonymous HESX1 Gene Mutation
AUTHORS: Coutinho, E; Brandao, CM; Lemos, MC;
PUBLISHED: 2019, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, VOLUME: 104, ISSUE: 7
INDEXED IN: WOS CrossRef: 6
IN MY: ORCID
24
TITLE: Bitter taste signaling mediated by Tas2r144 is down-regulated by 17β-estradiol and progesterone in the rat choroid plexus  Full Text
AUTHORS: Tomás, J; Santos, CRA; Duarte, AC; Maltez, M; Quintela, T; Lemos, MC; Gonçalves, I;
PUBLISHED: 2019, SOURCE: Molecular and Cellular Endocrinology, VOLUME: 495
INDEXED IN: Scopus CrossRef: 10
IN MY: ORCID
25
TITLE: Association of Vitamin D Pathway Genetic Variation and Thyroid Cancer
AUTHORS: Carvalho, IS; Goncalves, CI; Almeida, JT; Azevedo, T; Martins, T; Rodrigues, FJ; Lemos, MC;
PUBLISHED: 2019, SOURCE: GENES, VOLUME: 10, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 12
IN MY: ORCID
27
TITLE: Parathyroid identification by autofluorescence - preliminary report on five cases of surgery for primary hyperparathyroidism
AUTHORS: Serra, C; Silveira, L; Canudo, A; Lemos, MC;
PUBLISHED: 2019, SOURCE: BMC SURGERY, VOLUME: 19, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 13
IN MY: ORCID
28
TITLE: Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1 in juvenile diabetes
AUTHORS: Orabona, C; Mondanelli, G; Pallotta, MT; Carvalho, A; Albini, E; Fallarino, F; Vacca, C; Volpi, C; Belladonna, ML; Berioli, MG; Ceccarini, G; Esposito, SMR; Scattoni, R; Verrotti, A; Ferretti, A; De Giorgi, G; Toni, S; Cappa, M; Matteoli, MC; Bianchi, R; Matino, D; Iacono, A; Puccetti, M; Cunha, C; Bicciato, S; Antognelli, C; Talesa, VN; Chatenoud, L; Fuchs, D; Pilotte, L; Van den Eynde, B; Lemos, MC; Romani, L; Puccetti, P; Grohmann, U; ...More
PUBLISHED: 2018, SOURCE: JCI INSIGHT, VOLUME: 3, ISSUE: 6
INDEXED IN: WOS CrossRef: 48
IN MY: ORCID
29
TITLE: Association of FOXE1 polyalanine repeat region with thyroid cancer is dependent on tumour size
AUTHORS: Raimundo, J; Alvelos, MI; Azevedo, T; Martins, T; Rodrigues, FJ; Lemos, MC;
PUBLISHED: 2017, SOURCE: CLINICAL ENDOCRINOLOGY, VOLUME: 86, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 4
IN MY: ORCID
30
TITLE: Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism  Full Text
AUTHORS: Badiu, C; Bonomi, M; Borshchevsky, I; Cools, M; Craen, M; Ghervan, C; Hauschild, M; Hershkovitz, E; Hrabovszky, E; Juul, A; Kim, SH; Kumanov, P; Lecumberri, B; Lemos, MC; Neocleous, V; Niedziela, M; Djurdjevic, SP; Persani, L; Phan Hug, F; Pignatelli, D; Pitteloud, N; Popovic, V; Quinton, R; Skordis, N; Smith, N; Stefanija, MA; Xu, C; Young, J; Dwyer, AA; ...More
PUBLISHED: 2017, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 12, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 26
IN MY: ORCID
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